Advanced Master Program in Regulatory Affairs (12th edition)

Advanced Master Program in Regulatory Affairs (12th edition)

With a constantly evolving regulatory landscape, staying up to date is a necessity for medical professionals. This Master’s program is designed for those who wish to refine and specialize their skills to achieve a high level of expertise in regulatory activities applied to medical devices.

Date

7 May - 5 Nov, 2026

Registration Deadline

16 April, 2026

Format

Live Streaming

Language

Italian

Price

€3,700 for non Clients
€2,770 for Clients
(VAT excluded)

Download Brochure

The Master includes

Regulatory Affairs Toolkit (experiences, templates, and tools)
Support from an educational tutor
Educational materials
Competency assessments (for each lesson)
Pre-exam coaching session
Final exam discussion (thesis)
Certificate of Competence

Target Audience

Manufacturers
Authorized Representatives
Importers and Distributors
Consultants
PRRC – Art. 15 MDR (EU) 2017/745
Regulatory Affairs Professionals
Quality Management
Quality Assurance
R&D
Other Economic Operators

Certificates and Qualifications

The Master’s program awards a Certificate of Competence upon successful completion of the final exam.
AICQ Sicev Qualification

Benefits

Installment Plans
Option to pay the fee in installments according to an agreed plan.
Complimentary Invitation to MDG – MedGenerAction
Career Service
Collaboration with industry partners to create professional opportunities.
Team promotion
10% off for every extra participant from the same organization.